510(k) K013376 ยท DPW Flowmeter, Blood, Cardiovascular
QFLOW 500 PERFUSION MONITORING SYSTEM
| Applicant | Hemedex Incorporated, Hopkonton MA, US |
| Decision | Substantially Equivalent, May 8, 2002 |
| Received | Oct 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013376
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.